Incidental Mutation 'R2015:Mast3'
| ID |
222824 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Mast3
|
| Ensembl Gene |
ENSMUSG00000031833 |
| Gene Name |
microtubule associated serine/threonine kinase 3 |
| Synonyms |
|
| MMRRC Submission |
040024-MU
|
| Accession Numbers |
Ncbi RefSeq: NM_199308.2. MGI:2683541
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R2015 (G1)
|
| Quality Score |
186 |
|
Status
|
Not validated
|
| Chromosome |
8 |
| Chromosomal Location |
70778117-70805054 bp(-) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 70787363 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Phenylalanine
at position 338
(I338F)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000148686
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000166004]
[ENSMUST00000211948]
[ENSMUST00000212001]
[ENSMUST00000212038]
[ENSMUST00000212551]
[ENSMUST00000212673]
[ENSMUST00000212757]
[ENSMUST00000212875]
|
| AlphaFold |
Q3U214 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000166004
AA Change: I354F
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000128703
Gene: ENSMUSG00000031833
AA Change: I354F
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
43 |
59 |
N/A |
INTRINSIC |
|
Pfam:DUF1908
|
64 |
337 |
4.4e-128 |
PFAM |
|
S_TKc
|
373 |
646 |
2.77e-99 |
SMART |
|
S_TK_X
|
647 |
710 |
2.39e-1 |
SMART |
|
low complexity region
|
820 |
833 |
N/A |
INTRINSIC |
|
low complexity region
|
910 |
942 |
N/A |
INTRINSIC |
|
PDZ
|
958 |
1038 |
3.8e-15 |
SMART |
|
low complexity region
|
1053 |
1074 |
N/A |
INTRINSIC |
|
low complexity region
|
1089 |
1121 |
N/A |
INTRINSIC |
|
low complexity region
|
1124 |
1150 |
N/A |
INTRINSIC |
|
low complexity region
|
1180 |
1204 |
N/A |
INTRINSIC |
|
low complexity region
|
1231 |
1248 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000211841
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000211948
AA Change: I338F
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000212001
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000212038
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000212140
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000212551
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000212673
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000212757
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000212875
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.1%
- 20x: 94.7%
|
| Validation Efficiency |
|
| Allele List at MGI |
All alleles(2) : Targeted(1) Gene trapped(1)
|
| Other mutations in this stock |
Total: 94 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700006E09Rik |
C |
A |
11: 101,987,218 (GRCm38) |
H35Q |
probably damaging |
Het |
| 1700015F17Rik |
T |
A |
5: 5,455,964 (GRCm38) |
I106L |
probably benign |
Het |
| Abca9 |
A |
T |
11: 110,131,846 (GRCm38) |
M1022K |
probably benign |
Het |
| Abhd4 |
T |
A |
14: 54,262,832 (GRCm38) |
H74Q |
probably damaging |
Het |
| Actg1 |
A |
G |
11: 120,346,810 (GRCm38) |
S49P |
possibly damaging |
Het |
| Adcy8 |
C |
T |
15: 64,767,878 (GRCm38) |
G678S |
probably benign |
Het |
| Aire |
T |
C |
10: 78,042,958 (GRCm38) |
D85G |
probably damaging |
Het |
| Akr1c18 |
T |
A |
13: 4,145,309 (GRCm38) |
D50V |
probably damaging |
Het |
| Ankrd13a |
C |
A |
5: 114,792,109 (GRCm38) |
A185E |
probably damaging |
Het |
| Apc |
A |
G |
18: 34,315,591 (GRCm38) |
I1813V |
probably damaging |
Het |
| Armc8 |
A |
T |
9: 99,483,105 (GRCm38) |
C661* |
probably null |
Het |
| Bbs10 |
C |
T |
10: 111,300,855 (GRCm38) |
Q610* |
probably null |
Het |
| Blm |
T |
C |
7: 80,502,399 (GRCm38) |
E600G |
probably damaging |
Het |
| Bpifb9a |
T |
C |
2: 154,268,200 (GRCm38) |
|
probably null |
Het |
| Cdk14 |
T |
C |
5: 5,380,082 (GRCm38) |
K15R |
probably benign |
Het |
| Cdr1 |
A |
G |
X: 61,184,814 (GRCm38) |
F249L |
probably benign |
Het |
| Cep250 |
A |
C |
2: 155,981,453 (GRCm38) |
H1009P |
probably damaging |
Het |
| Clasp2 |
A |
G |
9: 113,911,500 (GRCm38) |
T495A |
possibly damaging |
Het |
| Col19a1 |
C |
G |
1: 24,559,753 (GRCm38) |
G53A |
unknown |
Het |
| Cpne1 |
G |
A |
2: 156,078,388 (GRCm38) |
R166C |
probably damaging |
Het |
| Dtx3l |
G |
A |
16: 35,936,427 (GRCm38) |
H129Y |
probably benign |
Het |
| Ercc3 |
A |
G |
18: 32,248,429 (GRCm38) |
T433A |
probably benign |
Het |
| Gm9936 |
T |
A |
5: 114,857,421 (GRCm38) |
|
probably benign |
Het |
| Grina |
T |
C |
15: 76,248,534 (GRCm38) |
V167A |
probably damaging |
Het |
| Hcfc2 |
A |
G |
10: 82,738,980 (GRCm38) |
N618D |
probably benign |
Het |
| Herpud1 |
T |
C |
8: 94,392,206 (GRCm38) |
V196A |
probably benign |
Het |
| Hist3h2a |
T |
A |
11: 58,954,928 (GRCm38) |
L64Q |
probably damaging |
Het |
| Hlcs |
A |
G |
16: 94,262,740 (GRCm38) |
V487A |
probably benign |
Het |
| Hspa9 |
A |
T |
18: 34,946,648 (GRCm38) |
Y243N |
probably damaging |
Het |
| Igll1 |
A |
G |
16: 16,863,775 (GRCm38) |
S39P |
probably benign |
Het |
| Kdm5a |
T |
C |
6: 120,431,990 (GRCm38) |
S1545P |
probably benign |
Het |
| Klra8 |
C |
A |
6: 130,115,573 (GRCm38) |
C255F |
probably damaging |
Het |
| Krtap4-6 |
A |
T |
11: 99,665,572 (GRCm38) |
C110S |
unknown |
Het |
| Lef1 |
T |
A |
3: 131,111,587 (GRCm38) |
I39N |
probably damaging |
Het |
| Lnpep |
G |
A |
17: 17,579,063 (GRCm38) |
T110I |
probably damaging |
Het |
| Lrp1 |
T |
A |
10: 127,540,694 (GRCm38) |
T4282S |
probably benign |
Het |
| Lrp6 |
A |
G |
6: 134,480,374 (GRCm38) |
|
probably null |
Het |
| Ly6g5b |
A |
C |
17: 35,114,678 (GRCm38) |
S53A |
possibly damaging |
Het |
| M6pr |
T |
G |
6: 122,313,373 (GRCm38) |
N98K |
probably damaging |
Het |
| Mal2 |
T |
C |
15: 54,600,740 (GRCm38) |
*176Q |
probably null |
Het |
| Mansc1 |
T |
C |
6: 134,610,311 (GRCm38) |
D301G |
possibly damaging |
Het |
| March1 |
C |
A |
8: 66,121,821 (GRCm38) |
N11K |
probably damaging |
Het |
| Mcm3 |
A |
G |
1: 20,803,580 (GRCm38) |
L772P |
probably damaging |
Het |
| Mib2 |
C |
T |
4: 155,657,880 (GRCm38) |
G176D |
probably damaging |
Het |
| Mier2 |
A |
T |
10: 79,541,202 (GRCm38) |
|
probably null |
Het |
| Mogs |
C |
T |
6: 83,117,650 (GRCm38) |
R483* |
probably null |
Het |
| Msl2 |
G |
T |
9: 101,075,251 (GRCm38) |
|
probably benign |
Het |
| Naa16 |
A |
T |
14: 79,345,059 (GRCm38) |
M530K |
probably damaging |
Het |
| Nde1 |
A |
T |
16: 14,169,457 (GRCm38) |
|
probably benign |
Het |
| Ndufb10 |
T |
C |
17: 24,722,529 (GRCm38) |
|
probably null |
Het |
| Nhsl1 |
A |
T |
10: 18,511,592 (GRCm38) |
R205W |
probably damaging |
Het |
| Npffr2 |
T |
A |
5: 89,582,892 (GRCm38) |
I227N |
probably damaging |
Het |
| Nup210l |
T |
A |
3: 90,185,432 (GRCm38) |
L1231Q |
probably damaging |
Het |
| Olfr1355 |
T |
C |
10: 78,879,388 (GRCm38) |
I72T |
possibly damaging |
Het |
| Olfr453 |
A |
G |
6: 42,744,850 (GRCm38) |
E271G |
probably damaging |
Het |
| Pclo |
C |
A |
5: 14,521,501 (GRCm38) |
P300Q |
probably damaging |
Het |
| Pik3c2a |
T |
A |
7: 116,350,931 (GRCm38) |
|
probably null |
Het |
| Plekha5 |
T |
A |
6: 140,534,564 (GRCm38) |
|
probably null |
Het |
| Pls1 |
A |
G |
9: 95,761,365 (GRCm38) |
V527A |
possibly damaging |
Het |
| Ppfia2 |
T |
C |
10: 106,474,677 (GRCm38) |
M15T |
probably benign |
Het |
| Prkd2 |
T |
A |
7: 16,847,677 (GRCm38) |
C152* |
probably null |
Het |
| Ptprq |
T |
G |
10: 107,667,422 (GRCm38) |
K792Q |
probably damaging |
Het |
| Rbbp8 |
T |
C |
18: 11,720,624 (GRCm38) |
M296T |
probably benign |
Het |
| Rfc3 |
T |
C |
5: 151,647,538 (GRCm38) |
|
probably null |
Het |
| Rnf17 |
A |
G |
14: 56,486,969 (GRCm38) |
N1090S |
probably benign |
Het |
| Sash1 |
A |
T |
10: 8,729,413 (GRCm38) |
V1071D |
probably benign |
Het |
| Sdsl |
G |
A |
5: 120,463,153 (GRCm38) |
T18M |
probably damaging |
Het |
| Sepsecs |
T |
A |
5: 52,647,624 (GRCm38) |
Q365L |
probably benign |
Het |
| Sgta |
A |
T |
10: 81,051,296 (GRCm38) |
V45E |
probably damaging |
Het |
| Slc25a46 |
A |
T |
18: 31,609,725 (GRCm38) |
H29Q |
probably benign |
Het |
| Slc2a8 |
A |
C |
2: 32,981,380 (GRCm38) |
V136G |
probably benign |
Het |
| Smg7 |
A |
T |
1: 152,860,508 (GRCm38) |
N166K |
probably damaging |
Het |
| Spata21 |
C |
T |
4: 141,107,329 (GRCm38) |
Q505* |
probably null |
Het |
| Strn4 |
T |
C |
7: 16,833,028 (GRCm38) |
S458P |
possibly damaging |
Het |
| Tbc1d22a |
C |
T |
15: 86,299,684 (GRCm38) |
T248M |
probably damaging |
Het |
| Trabd |
T |
A |
15: 89,084,726 (GRCm38) |
M149K |
possibly damaging |
Het |
| Trpv3 |
A |
T |
11: 73,279,827 (GRCm38) |
N178Y |
probably damaging |
Het |
| Try5 |
C |
T |
6: 41,314,651 (GRCm38) |
|
probably null |
Het |
| Tsg101 |
C |
T |
7: 46,908,904 (GRCm38) |
|
probably null |
Het |
| Ube3b |
A |
G |
5: 114,411,149 (GRCm38) |
E738G |
probably damaging |
Het |
| Unc13d |
A |
G |
11: 116,068,755 (GRCm38) |
S631P |
probably damaging |
Het |
| Unc5d |
T |
C |
8: 28,758,979 (GRCm38) |
T297A |
probably damaging |
Het |
| Usp18 |
A |
T |
6: 121,268,550 (GRCm38) |
E1V |
probably damaging |
Het |
| Vapb |
C |
A |
2: 173,771,598 (GRCm38) |
P97T |
probably benign |
Het |
| Vmn1r33 |
T |
A |
6: 66,612,372 (GRCm38) |
D66V |
probably benign |
Het |
| Vmn2r19 |
T |
A |
6: 123,315,995 (GRCm38) |
M332K |
probably benign |
Het |
| Vmn2r71 |
T |
A |
7: 85,620,637 (GRCm38) |
M452K |
probably benign |
Het |
| Vps13b |
T |
C |
15: 35,607,142 (GRCm38) |
S1074P |
probably damaging |
Het |
| Vwde |
C |
A |
6: 13,208,338 (GRCm38) |
G182C |
possibly damaging |
Het |
| Wdfy3 |
A |
C |
5: 101,860,486 (GRCm38) |
S2778A |
probably null |
Het |
| Zbtb2 |
T |
A |
10: 4,369,757 (GRCm38) |
I90F |
possibly damaging |
Het |
| Zfp518b |
C |
A |
5: 38,672,002 (GRCm38) |
V887F |
probably benign |
Het |
| Zfp790 |
A |
G |
7: 29,828,861 (GRCm38) |
T324A |
probably benign |
Het |
| Zufsp |
A |
G |
10: 33,929,824 (GRCm38) |
V437A |
possibly damaging |
Het |
|
| Other mutations in Mast3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00952:Mast3
|
APN |
8 |
70,780,683 (GRCm38) |
splice site |
probably benign |
|
|
IGL01411:Mast3
|
APN |
8 |
70,779,583 (GRCm38) |
missense |
possibly damaging |
0.50 |
|
IGL01475:Mast3
|
APN |
8 |
70,779,530 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL01886:Mast3
|
APN |
8 |
70,782,139 (GRCm38) |
missense |
possibly damaging |
0.94 |
|
IGL02104:Mast3
|
APN |
8 |
70,787,906 (GRCm38) |
missense |
possibly damaging |
0.78 |
|
IGL02236:Mast3
|
APN |
8 |
70,789,244 (GRCm38) |
missense |
probably benign |
0.36 |
|
IGL02437:Mast3
|
APN |
8 |
70,780,558 (GRCm38) |
missense |
possibly damaging |
0.79 |
|
IGL02704:Mast3
|
APN |
8 |
70,786,875 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL03155:Mast3
|
APN |
8 |
70,789,217 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL03366:Mast3
|
APN |
8 |
70,781,563 (GRCm38) |
nonsense |
probably null |
|
|
gravy
|
UTSW |
8 |
70,786,635 (GRCm38) |
missense |
probably damaging |
1.00 |
|
stuffing
|
UTSW |
8 |
70,784,797 (GRCm38) |
frame shift |
probably null |
|
|
turkey
|
UTSW |
8 |
70,785,482 (GRCm38) |
missense |
probably damaging |
1.00 |
|
BB010:Mast3
|
UTSW |
8 |
70,786,635 (GRCm38) |
missense |
probably damaging |
1.00 |
|
BB020:Mast3
|
UTSW |
8 |
70,786,635 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0037:Mast3
|
UTSW |
8 |
70,783,699 (GRCm38) |
critical splice donor site |
probably null |
|
|
R0280:Mast3
|
UTSW |
8 |
70,787,920 (GRCm38) |
missense |
possibly damaging |
0.65 |
|
R0280:Mast3
|
UTSW |
8 |
70,783,795 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0731:Mast3
|
UTSW |
8 |
70,781,321 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1101:Mast3
|
UTSW |
8 |
70,786,663 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1177:Mast3
|
UTSW |
8 |
70,780,324 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1208:Mast3
|
UTSW |
8 |
70,788,272 (GRCm38) |
splice site |
probably null |
|
|
R1208:Mast3
|
UTSW |
8 |
70,788,272 (GRCm38) |
splice site |
probably null |
|
|
R1333:Mast3
|
UTSW |
8 |
70,781,294 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1543:Mast3
|
UTSW |
8 |
70,792,311 (GRCm38) |
missense |
possibly damaging |
0.93 |
|
R1544:Mast3
|
UTSW |
8 |
70,786,172 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1738:Mast3
|
UTSW |
8 |
70,784,556 (GRCm38) |
missense |
probably benign |
0.38 |
|
R1842:Mast3
|
UTSW |
8 |
70,780,393 (GRCm38) |
missense |
possibly damaging |
0.91 |
|
R1936:Mast3
|
UTSW |
8 |
70,784,800 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2219:Mast3
|
UTSW |
8 |
70,780,963 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R2220:Mast3
|
UTSW |
8 |
70,780,963 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R3711:Mast3
|
UTSW |
8 |
70,779,607 (GRCm38) |
missense |
probably benign |
0.13 |
|
R3919:Mast3
|
UTSW |
8 |
70,779,422 (GRCm38) |
missense |
probably benign |
0.02 |
|
R4027:Mast3
|
UTSW |
8 |
70,787,908 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4060:Mast3
|
UTSW |
8 |
70,781,194 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4061:Mast3
|
UTSW |
8 |
70,781,194 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4062:Mast3
|
UTSW |
8 |
70,781,194 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4063:Mast3
|
UTSW |
8 |
70,781,194 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4588:Mast3
|
UTSW |
8 |
70,780,607 (GRCm38) |
nonsense |
probably null |
|
|
R4672:Mast3
|
UTSW |
8 |
70,784,797 (GRCm38) |
frame shift |
probably null |
|
|
R4770:Mast3
|
UTSW |
8 |
70,786,220 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4822:Mast3
|
UTSW |
8 |
70,780,366 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4830:Mast3
|
UTSW |
8 |
70,788,915 (GRCm38) |
missense |
possibly damaging |
0.87 |
|
R5196:Mast3
|
UTSW |
8 |
70,788,245 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5333:Mast3
|
UTSW |
8 |
70,783,501 (GRCm38) |
missense |
probably benign |
0.03 |
|
R5428:Mast3
|
UTSW |
8 |
70,784,733 (GRCm38) |
missense |
possibly damaging |
0.95 |
|
R5656:Mast3
|
UTSW |
8 |
70,786,221 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5920:Mast3
|
UTSW |
8 |
70,787,933 (GRCm38) |
missense |
probably benign |
0.00 |
|
R6177:Mast3
|
UTSW |
8 |
70,790,018 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6186:Mast3
|
UTSW |
8 |
70,785,483 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6407:Mast3
|
UTSW |
8 |
70,782,128 (GRCm38) |
missense |
probably benign |
0.02 |
|
R6614:Mast3
|
UTSW |
8 |
70,781,966 (GRCm38) |
missense |
possibly damaging |
0.95 |
|
R6804:Mast3
|
UTSW |
8 |
70,786,732 (GRCm38) |
missense |
probably benign |
0.29 |
|
R6873:Mast3
|
UTSW |
8 |
70,786,592 (GRCm38) |
nonsense |
probably null |
|
|
R6930:Mast3
|
UTSW |
8 |
70,799,471 (GRCm38) |
nonsense |
probably null |
|
|
R6948:Mast3
|
UTSW |
8 |
70,785,482 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7084:Mast3
|
UTSW |
8 |
70,779,473 (GRCm38) |
missense |
probably benign |
0.14 |
|
R7253:Mast3
|
UTSW |
8 |
70,789,682 (GRCm38) |
critical splice donor site |
probably null |
|
|
R7316:Mast3
|
UTSW |
8 |
70,779,788 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7357:Mast3
|
UTSW |
8 |
70,784,859 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7405:Mast3
|
UTSW |
8 |
70,786,171 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7429:Mast3
|
UTSW |
8 |
70,780,303 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7430:Mast3
|
UTSW |
8 |
70,780,303 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7521:Mast3
|
UTSW |
8 |
70,788,768 (GRCm38) |
missense |
probably benign |
0.16 |
|
R7576:Mast3
|
UTSW |
8 |
70,781,194 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7933:Mast3
|
UTSW |
8 |
70,786,635 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7998:Mast3
|
UTSW |
8 |
70,783,570 (GRCm38) |
missense |
probably benign |
|
|
R8021:Mast3
|
UTSW |
8 |
70,788,252 (GRCm38) |
missense |
probably benign |
0.02 |
|
R8204:Mast3
|
UTSW |
8 |
70,788,281 (GRCm38) |
missense |
probably benign |
0.00 |
|
R8327:Mast3
|
UTSW |
8 |
70,779,418 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8357:Mast3
|
UTSW |
8 |
70,780,441 (GRCm38) |
missense |
probably benign |
0.39 |
|
R8415:Mast3
|
UTSW |
8 |
70,781,222 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8457:Mast3
|
UTSW |
8 |
70,780,441 (GRCm38) |
missense |
probably benign |
0.39 |
|
R8530:Mast3
|
UTSW |
8 |
70,788,233 (GRCm38) |
missense |
possibly damaging |
0.92 |
|
R8891:Mast3
|
UTSW |
8 |
70,781,157 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8930:Mast3
|
UTSW |
8 |
70,781,733 (GRCm38) |
splice site |
probably benign |
|
|
R9002:Mast3
|
UTSW |
8 |
70,781,260 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9085:Mast3
|
UTSW |
8 |
70,796,717 (GRCm38) |
missense |
unknown |
|
|
R9087:Mast3
|
UTSW |
8 |
70,789,686 (GRCm38) |
missense |
possibly damaging |
0.93 |
|
R9148:Mast3
|
UTSW |
8 |
70,780,447 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R9364:Mast3
|
UTSW |
8 |
70,786,182 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9779:Mast3
|
UTSW |
8 |
70,785,483 (GRCm38) |
missense |
probably damaging |
1.00 |
|
Z1177:Mast3
|
UTSW |
8 |
70,789,038 (GRCm38) |
critical splice acceptor site |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- ATTACAGGCCAGTCCAGCTC -3'
(R):5'- GTTCAAAGACTCACTAGGGCTG -3'
Sequencing Primer
(F):5'- CAGCTCTCGGATACTTCTATGATGG -3'
(R):5'- CAAAGACTCACTAGGGCTGTTGTTTG -3'
|
| Posted On |
2014-08-25 |
Incidental Mutation